Male Urogenital Distress Inventory (MUDI): Difference between revisions
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=== Responsiveness === | === Responsiveness === | ||
=== Miscellaneous<span style="font-size: 20px; font-weight: normal | === Miscellaneous<span style="font-size: 20px; font-weight: normal" class="Apple-style-span"></span><br> === | ||
The MUDI captures the dimension of physical health, focusing on bother from multiple symptoms associated with urinary incontinence. | |||
Further testing should be done on test-retest reliability and sensitivity to change. Concurrent validity should also be evaluated further by comparing to a generic health-related quality of life instrument.<ref name="Robinson" /> | |||
== Links == | == Links == | ||
Revision as of 03:37, 16 February 2011
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Objective
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The Male Urogenital Distress Inventory (MUDI) can be used in clinical practice and research to measure the effect of interventions for urinary incontinence on health-related quality of life in men.[1]
Intended Population
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Community-dwelling, racially diverse men with continence problems.[1]
Method of Use[edit | edit source]
The MUDI contains 27 items that are each coded on the following 5-point scale: 1 = symptom not present, 2 = symptom present but not bothersome, 3 = symptom present and slightly bothersome, 4 = symptom present and moderately bothersome, and 5 = symptom present and greatly bothersome. Total scores range from 27 (no symptoms) to 135 (maximum degree of associated bother).[1]
It takes about 20 minutes to complete by either self-administration or interview.[1]
Reference
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Evidence[edit | edit source]
Reliability[edit | edit source]
Internal consistency score with Cronbach's coefficient was .89.[1]
Validity[edit | edit source]
Content validity agreement scores were 97% for item clarity and 95% for item fit.[1]
Responsiveness[edit | edit source]
Miscellaneous
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The MUDI captures the dimension of physical health, focusing on bother from multiple symptoms associated with urinary incontinence.
Further testing should be done on test-retest reliability and sensitivity to change. Concurrent validity should also be evaluated further by comparing to a generic health-related quality of life instrument.[1]
Links[edit | edit source]
Recent Related Research (from Pubmed)[edit | edit source]
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References[edit | edit source]
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